MAXISTIM— 510(k) K955031
Substantially EquivalentLife-Tech Intl., Inc.
FDA 510(k) clearance K955031 for MAXISTIM, Substantially Equivalent on 1996-12-10. Applicant: Life-Tech Intl., Inc.. Device class: 2.
Clearance details
- Applicant
- Life-Tech Intl., Inc.
- Product code
- Code KOI
- Device class
- Class 2
- Regulation
- 21 CFR 868.2775
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
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More clearances from Life-Tech Intl., Inc.
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